The Tage4 gene maps to rat chromosome 1q22

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Recommendations for a practical implementation of circulating tumor DNA mutation testing in metastatic non-small-cell lung cancer.

ESMO open·2022

Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.

Cancer genetics·2022

A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14).

Human genome variation·2020

Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients.

Genomics·2019

BENIGN AND PATHOLOGICAL GAIN OR LOSS OF GENETIC MATERIAL — ABOUT MICROSCOPIC AND SUBMICROSCOPIC COPY NUMBER VARIATIONS (CNVs) IN HUMAN GENETICS.

Tsitologiia·2018

Genome-wide characterization of copy number variations in Nagami Mithun (Bos frontalis) using whole-genome resequencing.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Screening for candidate genes and cell populations associated with atherosclerotic calcification using single-cell RNA sequencing.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Multi-omics analysis of HLTF context-dependent regulation across TCGA cohorts revealed its potential as new biomarker in tumour.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

The future objectives of the International Mouse Phenotyping Consortium (IMPC): functional evaluation of human disease-relevant cis-regulatory elements in the mouse genome.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Chiron3D: an interpretable deep learning framework for understanding the DNA code of chromatin looping.

Bioinformatics (Oxford, England)·2026

ARCADIA reveals spatially dependent transcriptional programs through integration of scRNA-seq and spatial proteomics.

Bioinformatics (Oxford, England)·2026

Massively parallel characterization of RNA G-quadruplex stability and molecular recognition.

Nucleic acids research·2026

Transcriptomic landscape of human circular RNAs: unveiling molecular mechanisms in high-altitude adaptation.

Frontiers in genetics·2026

DDX3X-mediated rRNA condensate clearance during germinal vesicle breakdown facilitates chromosome segregation in oocytes.

Biology of reproduction·2026

Inter-chromosomal Effect in a Robertsonian Translocation (13;14) Carrier with a Child Affected by Down Syndrome: A Case Report.

Journal of reproduction & infertility·2026

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The Tage4 gene maps to rat chromosome 1q22

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[Resistance to anti-EGFR through the successive and cumulative acquisition of two new oncogenic addictions: BRAF and ALK].

Recommendations for a practical implementation of circulating tumor DNA mutation testing in metastatic non-small-cell lung cancer.

Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.

A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14).

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